Eisspeedway

Thecachampsa

Thecachampsa
Temporal range: Miocene, 15.97–5.3 Ma[1]
T. carolinense skeleton
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Clade: Archosauromorpha
Clade: Archosauriformes
Order: Crocodilia
Superfamily: Gavialoidea
Family: Gavialidae
Subfamily: Tomistominae
Genus: Thecachampsa
Cope, 1867
Species

Thecachampsa is an extinct genus of gavialoid crocodylian, traditionally regarded as a member of the subfamily Tomistominae.[2] Fossils have been found from the eastern United States in deposits of Miocene age. Those named in the 19th century were distinguished primarily by the shape of their teeth, and have since been combined with T. antiquus. More recently erected species were reassigned from other genera, although their assignment to Thecachampsa has since been questioned.

Description

Thecachampsa, like other "tomistomines" of the Oligocene and Miocene, was considerably larger than living crocodilians. Like living gharials, it had a long, slender snout. The teeth were long and recurved. Unlike its living relatives, Thecachampsa was marine, inhabiting estuaries and shallow coastal waters. Other marine fossils such as sea snail and bivalve shells, shark teeth, and barnacles have been found alongside remains of Thecachampsa and similar taxa.[3]

Species

A vertebra in dorsal (top) and posterior (end) view, referred to Thecachampsa by William Bullock Clark in 1901
A tooth referred to Thecachampsa sericodon by William Bullock Clark in 1901

In 1852, American paleontologist Joseph Leidy described Crocodylus antiquus from Miocene deposits in the Lee family's ancestral home in Virginia.[4] The holotype was a tooth found in the Calvert Formation of Virginia. Leidy also described additional material including several teeth and osteoderms, two vertebrae, a rib, and an ungual phalanx or claw bone. The new genus Thecachampsa was erected by Edward Drinker Cope in 1867, containing two species, T. sericodon and T. contusor, both also based on teeth, but no type species was designated.[5] Cope (1882) designated T. sericodon as the Thecachampsa type species.[6] T. sericodon was distinguished from T. antiqua by its slender, curved teeth, each with a sharp edge near the base of the posterior margin (T. antiqua only possessed sharp edges along a small area near the tip of the posterior margin).[3]

Crocodilian material found from Miocene deposits in the eastern United States has often been attributed to Thecachampsa, even isolated teeth with few distinguishable features.[7] In 1869, Cope named a fourth species, T. sicaria, from a jaw fragment and a dorsal vertebra. Unlike those of other species, the teeth of T. sicaria were lenticular (lens-shaped) in cross section with sharp cutting edges.[3] That year, Othniel Charles Marsh named another species of Thecachampsa, "T. squankensis", after the place of its discovery, Squankum, New Jersey, but that name is a nomen nudum because Marsh provided no description, diagnosis, or type specimen.[8] Cope named a new species, T. fastigiata, in 1870 as a reassignment of Crocodylus fastigiatus, named by Leidy in 1852.[9] These species were distinguished from one another primarily by differences in the shape of the teeth, the most common material found. The genus was synonymized with Crocodylus in 1973, but has since been regarded as valid.[10]

A clear phylogenetic distinction between North American Gavialosuchus and the type species of Gavialosuchus, Gavialosuchus eggenburgensis Toula and Kail 1885[11] from the Miocene of Austria, was clear once they were analyzed together in phylogenetic analyses.[12][13][14][15] In 2001, A.C. Myrick synonymized Gavialosuchus americanus, another "tomistomine" from the eastern United States, with T. antiqua.[16] Myrick also synonymized Tomistoma lusitanicum, a "tomistomine" from Portugal, with Thecachampsa, though this has not been supported by subsequent analyses that clearly distinguish them.[13][14][15][17] The genus name Thecachampsa has priority over the other two, as it was erected earlier. A geologically younger species was first described from Florida as Tomistoma americanus in 1915, with remains having been found from the Kirkwood Formation in New Jersey, the Calvert Formation in Maryland, the Chesapeake Group of Virginia, and the Pungo River and Yorktown Formations of North Carolina. Remains have also been found from Florida, California, Baja California, and, more recently, Costa Rica. Fossils of the species are present in deposits that range in age from the late Early Miocene to the early Pliocene.[18] A few studies such as that of Jouve et al. (2008) have kept the species within Gavialosuchus, leaving T. antiqua as the only species within Thecachampsa,[19] though they didn't test Thecachampsa antiqua in their phylogenetic analysis, and most other analyses recover a clade including all North American forms that had previously been referred Gavialosuchus with a broad phylogenetic separation between them and G. eggenburgensis.[14][15][20][21]

The cladogram below follows from Brochu and Storrs (2012).

Coprolite attributed to Thecachampsa
Skull of T. americanus

In addition to reassigning G. americanus and G. carolinensis to Thecachampsa, Myrick combined all previously named species of Thecachampsa in a single species, with the oldest name being T. antiqua. The different tooth shapes that distinguished the species were considered variations in the dentition of a single species.[16] However, the variation in dentition could only be seen in complete skulls, all of which had been referred to Gavialosuchus before the genus was synonymized with Thecachampsa.

Weems (2018) agreed with Piras et al. (2007) and Brochu & Storrs (2012) that Tomistoma americana and Gavialosuchus carolinensis belong to Thecachampsa rather than Gavialosuchus, but treated sericodon and antiqua as distinct species rather than one species, and suggested that the americanus holotype is conspecific with T. sericodon, making T. americana a synonym of T. sericodon.

Most subsequent analyses have not accepted these suggestions based on clear differences between T. americana and T. antiqua and the lack of differences not explained by taphonomy between T. antiqua and T. sericodon.

Palaeoecology

Paired δ18O and δ13C measurements suggest that T. americana primarily fed on marine prey, in contrast to sympatric Alligator that ate freshwater prey.[22]

References

  1. ^ Rio, Jonathan P.; Mannion, Philip D. (6 September 2021). "Phylogenetic analysis of a new morphological dataset elucidates the evolutionary history of Crocodylia and resolves the long-standing gharial problem". PeerJ. 9: e12094. doi:10.7717/peerj.12094. PMC 8428266. PMID 34567843.
  2. ^ Iijima, M.; Kobayashi, Y. (2019). "Mosaic nature in the skeleton of East Asian crocodylians fills the morphological gap between "Tomistominae" and Gavialinae". Cladistics. 35 (6): 623–632. doi:10.1111/cla.12372. PMID 34618925. S2CID 91400957.
  3. ^ a b c Cope, E.D. (1871). "Crocodilia". Synopsis of the Extinct Batrachia and Reptilia of North America. Transactions of the American Philosophical Society. American Philosophical Society. pp. 61–82.
  4. ^ Leidy, J. (1852). "Description of a new species of crocodile from the Miocene of Virginia". Journal of the Academy of Natural Sciences of Philadelphia. 2: 135–138.
  5. ^ Cope, E.D. (1867). "Note on Thoracosaurus brevispinus". Proceedings of the Academy of Natural Sciences of Philadelphia. 19: 39.
  6. ^ Cope, E. D. 1882. The Reptiles of the American Eocene. American Naturalist, 16:979–993. https://doi.org/10.1086/273224.
  7. ^ Holman, J.A. (1998). "Geology and paleontology of the lower Miocene Pollack Farm Fossil Site, Delaware". In Benson, R.N. (ed.). Delaware Geological Survey Special Publication No. 21. pp. 141–147.
  8. ^ Marsh, Othniel C. (1869). "Notice of some new reptilian remains from the Cretaceous of Brazil". American Journal of Science. 47 (141).
  9. ^ Spamer, E.E.; Daeschler, E.; Vostreys-Shapiro, L.G. (1995). A Study of Fossil Vertebrate Types in the Academy of Natural Sciences of Philadelphia: Taxonomic, Systematic, and Historical Perspectives. Philadelphia: Academy of Natural Sciences. p. 120.
  10. ^ Steel, R. (1973). "Crocodylia". Handbuch der Paläoherpetologie. Vol. 16. Stuttgart: Gustav Fischer Verlag. p. 116.
  11. ^ Toula, F.; Kail, J.A. (1885). "Uber einen Krokodil-Schadel aus den Tertiärablagerungen von Eggenburg in Niederosterreich: eine palaontologische Studie". Denkschriften der kaiserlichen Akademie der Wissenschaften Mathematisch-Naturwissenschaftliche Classe. 50: 299–355.
  12. ^ Brochu, C.A.; Gingerich, P.D. (2000). "New tomistomine crocodylian from the middle Eocene (Bartonian) of Wadi Hitan, Fayum Province, Egypt". Contributions from the Museum of Paleontology, University of Michigan. 30: 251–268.
  13. ^ a b Piras, P.; Delfino, M.; Del Favero, L.; Kotsakis, T. (2007). "Phylogenetic position of the crocodylian Megadontosuchus arduini and tomistomine palaeobiogeography" (PDF). Acta Palaeontologica Polonica. 52 (2): 315–328.
  14. ^ a b c Shan, Hsi-yin; Wu, Xiao-chun; Cheng, Yen-nien; Sato, Tamaki (2009). "A new tomistomine (Crocodylia) from the Miocene of Taiwan". Canadian Journal of Earth Sciences. 46 (7): 529–555. Bibcode:2009CaJES..46..529S. doi:10.1139/E09-036.
  15. ^ a b c Brochu, C. A.; Storrs, G. W. (2012). "A giant crocodile from the Plio-Pleistocene of Kenya, the phylogenetic relationships of Neogene African crocodylines, and the antiquity of Crocodylus in Africa". Journal of Vertebrate Paleontology. 32 (3): 587. doi:10.1080/02724634.2012.652324. S2CID 85103427.
  16. ^ a b Myrick, A.C. (2001). "Thecachampsa antiqua (Leidy, 1852) (Crocodylidae: Thoracosaurinae) from fossil marine deposits at Lee Creek Mine, Aurora, North Carolina, USA". Smithsonian Contributions to Paleobiology. 90: 219–225.
  17. ^ Ristevski, Jorgo; Price, G.J.; Weisbecker, V.; Salisbury, S.W. (2021). "First record of a tomistomine crocodylian from Australia". Scientific Reports. 11 (2): 12158. doi:10.1038/s41598-021-91717-y. PMC 8190066.
  18. ^ Laurito, C.A.; Valerio, A.L. (2009). "The first record of Gavialosuchus americanus Sellards (1915) (Eusuchia: Crocodylidae, Tomistominae) for the Late Tertiary of Costa Rica and Central America" (PDF). Revista Geólogica de América Central. 39: 107–115. ISSN 0256-7024. Archived from the original (PDF) on 2011-07-18.
  19. ^ Jouve, S.; Bardet, N.; Jalil, N.-E.; Suberbiola, X.P.; Bouya, B.; Amaghzaz, M. (2008). "The oldest African crocodylian: phylogeny, paleobiogeography, and differential survivorship of marine reptiles through the Cretaceous-Tertiary boundary" (PDF). Journal of Vertebrate Paleontology. 28 (2): 409–421. doi:10.1671/0272-4634(2008)28[409:TOACPP]2.0.CO;2. S2CID 86503283.
  20. ^ Rio, Jonathan P.; Mannion, Philip D. (6 September 2021). "Phylogenetic analysis of a new morphological dataset elucidates the evolutionary history of Crocodylia and resolves the long-standing gharial problem". PeerJ. 9: e12094. doi:10.7717/peerj.12094. PMC 8428266. PMID 34567843.
  21. ^ Nicholl, Cecily S.C.; Rio, J.P.; Mannion, P.D.; Delfino, M. "A re-examination of the anatomy and systematics of the tomistomine crocodylians from the Miocene of Italy and Malta". Journal of Systematic Palaeontology. 18: 1853–1889.
  22. ^ Whiting, Evan T.; Steadman, David W.; Krigbaum, John (1 June 2016). "Paleoecology of Miocene crocodylians in Florida: Insights from stable isotope analysis". Palaeogeography, Palaeoclimatology, Palaeoecology. 451: 23–34. doi:10.1016/j.palaeo.2016.03.009. Retrieved 18 November 2024 – via Elsevier Science Direct.